rs900755711 Rat Genome Database

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Variant: rs900755711 -  Homo sapiens

RGD ID: 13534682
RS ID: rs900755711
ClinVar ID: CV501653
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: SERAC1  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 6 158,589,177
GRCh38 6 158,168,145
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NR_073096.2:n.118C>T
NG_032889.1:g.5136C>T
NC_000006.12:g.158168145G>A
NC_000006.11:g.158589177G>A
More... 		11/10/2017 5 prime utr variant likely benign AllHighlyPenetrant

Variant Details
Variant Transcripts
Gene Symbol:SERAC1
Accession:XM_047419421
Location:5UTRS;EXON

Gene Symbol:SERAC1
Accession:NM_032861
Location:5UTRS;EXON

Gene Symbol:SERAC1
Accession:XM_006715586
Location:5UTRS;EXON

Gene Symbol:SERAC1
Accession:NR_073096
Location:EXON;NON-CODING

Gene Symbol:SERAC1
Accession:XM_024446573
Location:INTRON

Gene Symbol:SERAC1
Accession:XM_011536198
Location:INTRON

Gene Symbol:SERAC1
Accession:XR_007059349
Location:INTRON;NON-CODING

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000601969 CLINVAR
dbSNP (RS) rs900755711 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene SERAC1 CLINVAR
OMIM 614725 CLINVAR